A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1090590



Internal ID15943776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:93909769..93913138hg38UCSC Ensembl
Innerchr7:93539081..93542450hg19UCSC Ensembl
Innerchr7:93377017..93380386hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg383370
hg193370
hg183370
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607851
Supporting Variants
Samples
Known GenesGNGT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1090590
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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